VEGGIOTTI, PIERANGELO
VEGGIOTTI, PIERANGELO
Dipartimento di Scienze Biomediche e Cliniche
Thyroid dysfunction in children and adolescents affected by undernourished and overnourished eating disorders
2023 V. Calcaterra, V.C. Magenes, F. Siccardo, C. Hruby, M. Basso, V. Conte, G. Maggioni, V. Fabiano, S. Russo, P. Veggiotti, G. Zuccotti
Menkes disease complicated by concurrent ACY1 deficiency: A case report
2023 A. Mauri, L.A. Saielli, E. Alfei, M. Iascone, D. Marchetti, E. Cattaneo, A. Di Lauro, L. Antonelli, L. Alberti, E. Bonaventura, P. Veggiotti, L. Spaccini, C. Cereda
FDXR-associated disease: a challenging differential diagnosis with inflammatory peripheral neuropathy
2023 S. Masnada, R. Previtali, P. Erba, E. Beretta, A. Camporesi, L. Chiapparini, C. Doneda, M. Iascone, M.U.A. Sartorio, L. Spaccini, P. Veggiotti, M. Osio, D. Tonduti, I. Moroni
Long-term follow-up of nutritional status in children with GLUT1 Deficiency Syndrome treated with classic ketogenic diet: a 5-year prospective study
2023 R. De Amicis, A. Leone, M. Pellizzari, A. Foppiani, A. Battezzati, C. Lessa, A. Tagliabue, C. Ferraris, V. De Giorgis, S. Olivotto, R. Previtali, P. Veggiotti, S. Bertoli
Newborn screening for X-linked adrenoleukodystrophy in Italy: Diagnostic algorithm and disease monitoring
2023 E. Bonaventura, L. Alberti, S. Lucchi, L. Cappelletti, S. Fazzone, E. Cattaneo, M. Bellini, G. Izzo, C. Parazzini, A. Bosetti, E. Di Profio, G. Fiore, M. Ferrario, C. Mameli, A. Sangiorgio, S. Masnada, G.V. Zuccotti, P. Veggiotti, L. Spaccini, M. Iascone, E. Verduci, C. Cereda, D. Tonduti
Extended Glasgow Outcome Scale to Evaluate the Functional Impairment of Patients With Subcortical Band Heterotopia: A Multicentric Cross-sectional Study
2023 I. Toldo, F. Brunello, P. Cavasin, M. Nosadini, S. Sartori, A.C. Frigo, R. Mai, V. Pelliccia, M.M. Mancardi, P. Striano, M. Severino, F. Zara, R. Rizzi, S. Casellato, G. Di Rosa, M. Mastrangelo, A. Spalice, M. Budetta, L. De Palma, R. Guerrini, D. Pruna, D.M. Cordelli, V. Sofia, A. Papa, V. Chiesa, F. Ragona, P. Parisi, A. D'Aniello, P. Veggiotti, F. Dainese, L. Giordano, L. Licchetta, P. Tinuper, G. D'Orsi, M. Cassina, R. Manara
GLUT1-DS Italian registry: past, present, and future: a useful tool for rare disorders
2023 C. Varesio, V. De Giorgis, P. Veggiotti, N. Nardocci, T. Granata, F. Ragona, L. Pasca, M.M. Mensi, R. Borgatti, S. Olivotto, R. Previtali, A. Riva, M.M. Mancardi, P. Striano, M. Cavallin, R. Guerrini, F.F. Operto, A. Pizzolato, R. Di Maulo, F. Martino, A. Lodi, C. Marini
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications
2022 K.M. Johannesen, Y. Liu, M. Koko, C.E. Gjerulfsen, L. Sonnenberg, J. Schubert, C.D. Fenger, A. Eltokhi, M. Rannap, N.A. Koch, S. Lauxmann, J. Krüger, J. Kegele, L. Canafoglia, S. Franceschetti, T. Mayer, J. Rebstock, P. Zacher, S. Ruf, M. Alber, K. Sterbova, P. Lassuthová, M. Vlckova, J.R. Lemke, K. Platzer, I. Krey, C. Heine, D. Wieczorek, J. Kroell-Seger, C. Lund, K.M. Klein, P.Y.B. Au, J.M. Rho, A.W. Ho, S. Masnada, P. Veggiotti, L. Giordano, P. Accorsi, C.E. Hoei-Hansen, P. Striano, F. Zara, H. Verhelst, J.S. Verhoeven, H.M.H. Braakman, B. van der Zwaag, A.V.E. Harder, E. Brilstra, M. Pendziwiat, S. Lebon, M. Vaccarezza, N.M. Le, J. Christensen, S. Grønborg, S.W. Scherer, J. Howe, W. Fazeli, K.B. Howell, R. Leventer, C. Stutterd, S. Walsh, M. Gerard, B. Gerard, S. Matricardi, C.M. Bonardi, S. Sartori, A. Berger, D. Hoffman-Zacharska, M. Mastrangelo, F. Darra, A. Vøllo, M.M. Motazacker, P. Lakeman, M. Nizon, C. Betzler, C. Altuzarra, R. Caume, A. Roubertie, P. Gélisse, C. Marini, R. Guerrini, F. Bilan, D. Tibussek, M. Koch-Hogrebe, M.S. Perry, S. Ichikawa, E. Dadali, A. Sharkov, I. Mishina, M. Abramov, I. Kanivets, S. Korostelev, S. Kutsev, K.E. Wain, N. Eisenhauer, M. Wagner, J.M. Savatt, K. Müller-Schlüter, H. Bassan, A. Borovikov, M.C. Nassogne, A. Destrée, A.S. Schoonjans, M. Meuwissen, M. Buzatu, A. Jansen, E. Scalais, S. Srivastava, W.H. Tan, H.E. Olson, T. Loddenkemper, A. Poduri, K.L. Helbig, I. Helbig, M.P. Fitzgerald, E.M. Goldberg, T. Roser, I. Borggraefe, T. Brünger, P. May, D. Lal, D. Lederer, G. Rubboli, H.O. Heyne, G. Lesca, U.B.S. Hedrich, J. Benda, E. Gardella, H. Lerche, R.S. Møller
EEG at onset and MRI predict long-term clinical outcome in Aicardi syndrome
2022 S. Masnada, E. Alfei, M. Formica, R. Previtali, P. Accorsi, F. Arrigoni, P. Bonanni, R. Borgatti, F. Darra, C. Fusco, V. De Giorgis, L. Giordano, F. La Briola, S. Orcesi, E. Osanni, C. Parazzini, L. Pinelli, E. Rebessi, R. Romaniello, A. Romeo, C. Spagnoli, C. Uebler, C. Varesio, M. Viri, C. Zucca, A. Pichiecchio, P. Veggiotti
A complex epileptic and dysmorphic phenotype associated with a novel frameshift KDM5B variant and deletion of SCN gene cluster
2022 G.D. Mangano, V. Antona, E. Cali, A. Fontana, V. Salpietro, H. Houlden, P. Veggiotti, R. Nardello
Cognitive, Behavioral and Socioemotional Development in a Cohort of Preterm Infants at School Age: A Cross-Sectional Study
2022 C. Ionio, G. Lista, P. Veggiotti, C. Colombo, G. Ciuffo, I. Daniele, M. Landoni, B. Scelsa, E. Alfei, S. Bova
Connections Between Febrile Infection-Related Epilepsy Syndrome and Autoimmune Encephalitis. A Case Report of a Child With New Anti-neuronal Antibodies
2022 M. Basso, M. Gastaldi, V. Leonardi, G. Izzo, S. Olivotto, S. Ferrario, P. Veggiotti, D. Franciotta, S.M. Bova
Neurological Involvement in Multisystem Inflammatory Syndrome in Children: Clinical, Electroencephalographic and Magnetic Resonance Imaging Peculiarities and Therapeutic Implications. An Italian Single-Center Experience
2022 S.M. Bova, L. Serafini, P. Capetti, A.R. Dallapiccola, C. Doneda, A. Gadda, L. Lonoce, A. Vittorini, S. Mannarino, P. Veggiotti
Seizures may be an early sign of acute COVID-19, and the Omicron variant could present a more epileptogenic profile
2022 S.M. Bova, L. Serafini, I. Serati, L. Fiori, P. Veggiotti
Sex-dependent association between variability in infants’ OXTR methylation at birth and negative affectivity at 3 months
2022 S. Nazzari, S. Grumi, M. Villa, F. Mambretti, G. Biasucci, L. Decembrino, R. Giacchero, M.L. Magnani, R. Nacinovich, F. Prefumo, A. Spinillo, P. Veggiotti, E. Fullone, R. Giorda, L. Provenzi
Long-term therapeutic effect of eslicarbazepine acetate in children: An open-label extension of a cognition study in children aged 6–16 years
2022 P. Veggiotti, S. Jozwiak, F. Kirkham, J. Moreira, A. Pereira, F. Ikedo, H. Gama
Successful use of perampanel in GABRA1-related myoclonic epilepsy with photosensitivity
2022 S. Olivotto, A. Freddi, R. Lavatelli, E. Basso, A. Leidi, B. Castellotti, L. Spaccini, S.M. Bova, P. Veggiotti
Glut1 deficiency syndrome throughout life: clinical phenotypes, intelligence, life achievements and quality of life in familial cases
2022 S. Olivotto, A. Duse, S. Maria Bova, V. Leonardi, E. Biganzoli, A. Milanese, C. Cereda, S. Bertoli, R. Previtali, P. Veggiotti
Safety and efficacy of ganaxolone in patients with CDKL5 deficiency disorder: results from the double-blind phase of a randomised, placebo-controlled, phase 3 trial
2022 E.M.P. Knight, S. Amin, N. Bahi-Buisson, T.A. Benke, J.H. Cross, S.T. Demarest, H.E. Olson, N. Specchio, T.R. Fleming, A.A. Aimetti, M. Gasior, O. Devinsky, E. Belousova, O. Belyaev, B. Ben-Zeev, A. Brunklaus, M.A. Ciliberto, F. Darra, R. Davis, V. De Giorgis, O. Doronina, M. Fahey, R. Guerrini, P. Heydemann, O. Khaletskaya, P. Lisewski, E.D. Marsh, A.N. Moosa, S. Perry, S. Philip, R.R. Rajaraman, B. Renfroe, R.P. Saneto, I.E. Scheffer, Y. Sogawa, B. Suter, M.T. Sweney, D. Tarquinio, P. Veggiotti, G. Wallace, J. Weisenberg, A. Wilfong, E.C. Wirrell, M. Zafar, M. Zolnowska
Exclusive breastfeeding and maternal postnatal anxiety contributed to infants' temperament issues at 6 months of age
2022 S. Grumi, E. Capelli, R. Giacchero, G. Anceresi, E. Fullone, L. Provenzi, G. Bensi, G. Biasucci, A. Cavallini, L. Decembrino, R. Falcone, E. Fazzi, B. Gardella, R. Longo, M.L. Magnani, R. Nacinovich, D. Pantaleo, B. Pietra, C. Pisoni, F. Prefumo, B. Scelsa, P. Veggiotti